205686009: Karyotype 46, X iso (Xq) (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Karyotype 46, X iso (Xq)
• \Anomaly of chromosome X\Turner syndrome\Karyotype 46, X iso (Xq)
• \Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Karyotype 46, X iso (Xq)
• \Anomaly of chromosome X\Turner syndrome\Karyotype 46, X iso (Xq)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315437010	Karyotype 46, X iso (Xq)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
591088014	Karyotype 46, X iso (Xq) (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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